Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 345081017 | Silver disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core | 
| 618047012 | Silver disease (disorder) | en | Fully specified name | Inactive | Entire term case insensitive (core metadata concept) | SNOMED CT core | 
| 3701800010 | Autosomal dominant spastic paraplegia type 17 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | 
| 3701801014 | Autosomal dominant spastic paraplegia type 17 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | 
| 4674028016 | A complex hereditary spastic paraplegia with characteristics of progressive spastic paraplegia, upper and lower limb muscle atrophy, hyperreflexia, extensor plantar responses, pes cavus and occasionally impaired vibration sense. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core | 
| 3613841000052118 | Silvers sjukdom | sv | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) | 
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values | 
| Autosomal dominant spastic paraplegia type 17 (disorder) | Is a | sjukdom som primärt påverkar motoriska banor | false | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Structure of nervous system (body structure) | false | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Lower limb structure | true | Inferred relationship | Some | 2 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Is a | Autosomal dominant hereditary spastic paraplegia | true | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Spinal cord structure | true | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Associated morphology | degeneration | false | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Associated morphology | Degenerative abnormality (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Peripheral nervous system structure | true | Inferred relationship | Some | 3 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Is a | Autosomal dominant distal hereditary motor neuropathy (disorder) | true | Inferred relationship | Some | ||
| Autosomal dominant spastic paraplegia type 17 (disorder) | Finding site | Nerve structure | true | Inferred relationship | Some | 4 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 5 | |
| Autosomal dominant spastic paraplegia type 17 (disorder) | Is a | Complicated hereditary spastic paraplegia | true | Inferred relationship | Some | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
This concept is not in any reference sets